HazMat Fee +
There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| Type | HazMat fee for 500 gram (Estimated) |
| Excepted Quantity | USD 0.00 |
| Limited Quantity | USD 15-60 |
| Inaccessible (Haz class 6.1), Domestic | USD 80+ |
| Inaccessible (Haz class 6.1), International | USD 150+ |
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |
Structure of NEPA
CAS No.: 82717-96-2
*Storage: {[sel_prStorage]}
*Shipping: {[sel_prShipping]}
The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Synonyms: (S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoic acid
4.5
*For Research Use Only! Not for Human Use. We Do Not Sell to Patients.
Change View
| Size | Price | VIP Price |
DE Stock US Stock |
Asia Stock Global Stock |
In Stock |
| {[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} |
Inquiry
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.discount_usd) ]} {[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} |
Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]} | {[ item.p_spot_brand_remark ]} 1-2 weeks {[ item.pr_usastock ]} In Stock Inquiry - | {[ item.p_spot_brand_remark ]} 1-2 weeks {[ item.pr_chinastock ]} {[ item.pr_remark ]} In Stock Inquiry - | Login - + |
Please Login or Create an Account to: See VIP prices and availability
Asia Stock: Ship in 3-5 business days
EU Stock: ship in 0-1 business day
Global Stock: ship in 7-10 days
US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days
{[ item.p_spot_brand_remark ]}
1-2weeks
Inquiry
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd,1,item.mem_rate,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ item.p_spot_brand_remark ]}
1-2weeks
Inquiry
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
In Stock
- +
Please Login or Create an Account to: See VIP prices and availability
Asia Stock: Ship in 3-5 business days
EU Stock: ship in 0-1 business day
Global Stock: ship in 7-10 days
US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
| CAS No. : | 82717-96-2 |
| Formula : | C15H21NO4 |
| M.W : | 279.33 |
| SMILES Code : | C[C@H](N[C@@H](CCC1=CC=CC=C1)C(OCC)=O)C(O)=O |
| Synonyms : |
(S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoic acid
|
| English Name : | (S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoic acid |
| MDL No. : | MFCD00209976 |
| InChI Key : | CEIWXEQZZZHLDM-AAEUAGOBSA-N |
| Pubchem ID : | 5702571 |
| GHS Pictogram: | |
| Signal Word: | |
| Hazard Statements: | |
| Precautionary Statements: | |
| Class: | |
| UN#: | |
| Packing Group: |
| Num. heavy atoms | 20 |
| Num. arom. heavy atoms | 6 |
| Fraction Csp3 | 0.47 |
| Num. rotatable bonds | 9 |
| Num. H-bond acceptors | 5.0 |
| Num. H-bond donors | 2.0 |
| Molar Refractivity | 75.72 |
| TPSA ? Topological Polar Surface Area: Calculated from |
75.63 Ų |
| Log Po/w (iLOGP)? iLOGP: in-house physics-based method implemented from |
2.44 |
| Log Po/w (XLOGP3)? XLOGP3: Atomistic and knowledge-based method calculated by |
0.15 |
| Log Po/w (WLOGP)? WLOGP: Atomistic method implemented from |
1.61 |
| Log Po/w (MLOGP)? MLOGP: Topological method implemented from |
-0.4 |
| Log Po/w (SILICOS-IT)? SILICOS-IT: Hybrid fragmental/topological method calculated by |
2.19 |
| Consensus Log Po/w? Consensus Log Po/w: Average of all five predictions |
1.2 |
| Log S (ESOL):? ESOL: Topological method implemented from |
-1.29 |
| Solubility | 14.2 mg/ml ; 0.0508 mol/l |
| Class? Solubility class: Log S scale |
Very soluble |
| Log S (Ali)? Ali: Topological method implemented from |
-1.3 |
| Solubility | 14.2 mg/ml ; 0.0507 mol/l |
| Class? Solubility class: Log S scale |
Very soluble |
| Log S (SILICOS-IT)? SILICOS-IT: Fragmental method calculated by |
-3.6 |
| Solubility | 0.071 mg/ml ; 0.000254 mol/l |
| Class? Solubility class: Log S scale |
Soluble |
| GI absorption? Gatrointestinal absorption: according to the white of the BOILED-Egg |
High |
| BBB permeant? BBB permeation: according to the yolk of the BOILED-Egg |
No |
| P-gp substrate? P-glycoprotein substrate: SVM model built on 1033 molecules (training set) |
No |
| CYP1A2 inhibitor? Cytochrome P450 1A2 inhibitor: SVM model built on 9145 molecules (training set) |
No |
| CYP2C19 inhibitor? Cytochrome P450 2C19 inhibitor: SVM model built on 9272 molecules (training set) |
No |
| CYP2C9 inhibitor? Cytochrome P450 2C9 inhibitor: SVM model built on 5940 molecules (training set) |
No |
| CYP2D6 inhibitor? Cytochrome P450 2D6 inhibitor: SVM model built on 3664 molecules (training set) |
No |
| CYP3A4 inhibitor? Cytochrome P450 3A4 inhibitor: SVM model built on 7518 molecules (training set) |
No |
| Log Kp (skin permeation)? Skin permeation: QSPR model implemented from |
-7.9 cm/s |
| Lipinski? Lipinski (Pfizer) filter: implemented from |
0.0 |
| Ghose? Ghose filter: implemented from |
None |
| Veber? Veber (GSK) filter: implemented from |
0.0 |
| Egan? Egan (Pharmacia) filter: implemented from |
0.0 |
| Muegge? Muegge (Bayer) filter: implemented from |
0.0 |
| Bioavailability Score? Abbott Bioavailability Score: Probability of F > 10% in rat |
0.55 |
| PAINS? Pan Assay Interference Structures: implemented from |
0.0 alert |
| Brenk? Structural Alert: implemented from |
0.0 alert: heavy_metal |
| Leadlikeness? Leadlikeness: implemented from |
No; 1 violation:MW<1.0 |
| Synthetic accessibility? Synthetic accessibility score: from 1 (very easy) to 10 (very difficult) |
2.81 |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| In tetrahydrofuran; toluene for 2.5h; Heating; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| Multi-step reaction with 5 steps 1: CoCl2 / H2O / 72 h / 37 °C / aminoacylase (from Aspergillus oryzae); pH 7 2: SOCl2 3: 43.6 percent / K2CO3 / dimethylsulfoxide / 30 h / Ambient temperature 4: ethyl acetate; diisopropyl ether 5: 96 percent / H2 / Pd / ethanol / 3 h / 760 Torr / Ambient temperature |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| Multi-step reaction with 3 steps 1: 1->3-(dimethylamino)propyl>-3-ethylcarbodiimide hydrochloride / dimethylformamide / 18 h / Ambient temperature 2: 4.6 g / NEt3 / dimethylformamide / Ambient temperature 3: 0.4 g / conc. aq. HCl / acetonitrile / 10 h / 5 °C | ||
| Multi-step reaction with 2 steps 1: 1.) N,N-disuccinimidyl carbonate, pyridine, 2.) NEt3 / 1.) CH3CN, RT, 44 h, 2.) CH3CN, H2O, RT 2: 0.4 g / conc. aq. HCl / acetonitrile / 10 h / 5 °C |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| Multi-step reaction with 3 steps 1: 43.6 percent / K2CO3 / dimethylsulfoxide / 30 h / Ambient temperature 2: ethyl acetate; diisopropyl ether 3: 96 percent / H2 / Pd / ethanol / 3 h / 760 Torr / Ambient temperature |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 1: 14 %Chromat. 2: 0.5 %Chromat. 3: 0.4 %Chromat. 4: 0.5 %Chromat. | Stage #1: N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanine N-carboxyanhydride; <i>L</i>-proline In water; ethyl acetate at 19 - 20℃; for 5h; Stage #2: at 30℃; for 0.166667h; | |
| 1: 10 %Chromat. 2: 0.6 %Chromat. 3: 0.5 %Chromat. 4: 0.5 %Chromat. | Stage #1: N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanine N-carboxyanhydride; <i>L</i>-proline In dichloromethane; water at 19 - 20℃; for 5h; Stage #2: at 30℃; for 0.166667h; | |
| 1: 14 %Chromat. 2: 0.4 %Chromat. 3: 0.5 %Chromat. 4: 0.6 %Chromat. | Stage #1: N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanine N-carboxyanhydride; <i>L</i>-proline In water; ethyl acetate at 19 - 20℃; for 5h; Stage #2: at 30℃; for 0.166667h; |
| 1: 18 %Chromat. 2: 0.05 %Chromat. 3: 0.4 %Chromat. 4: 0.7 %Chromat. | Stage #1: N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanine N-carboxyanhydride; <i>L</i>-proline In water at 19 - 20℃; for 6h; Stage #2: at 30℃; for 0.166667h; | |
| 1: 18 %Chromat. 2: 0.05 %Chromat. 3: 0.1 %Chromat. 4: 0.6 %Chromat. | Stage #1: N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanine N-carboxyanhydride; <i>L</i>-proline In water at 14 - 15℃; for 9h; Stage #2: at 30℃; for 0.166667h; | |
| 1: 21 %Chromat. 2: 0.05 %Chromat. 3: 0.4 %Chromat. 4: 0.6 %Chromat. | Stage #1: N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanine N-carboxyanhydride; <i>L</i>-proline In dihydrogen peroxide at 19 - 20℃; for 7h; Stage #2: at 30℃; for 0.166667h; |

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 80% | Stage #1: bis(trichloromethyl) carbonate With tributyl-amine In toluene for 0.0166667h; Stage #2: [1(S)-(ethoxycarbonyl)-3-phenylpropyl]-(S)-alanine With tributyl-amine In tetrahydrofuran; toluene for 0.05h; | 7; 2 Example 7 To 0.64 g of triphosgene, 3.38 g of toluene was added to prepare a homogeneous solution, and the resulting solution was referred to as a raw material liquid A. To 0.40 g of tributylamine, 3.62 g of toluene was added to prepare a homogeneous solution, and the resulting solution was referred to as a raw material liquid B. To 1.50 g of N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanine and 1.09 g of tributylamine, 13.50 g of tetrahydrofuran was added to prepare a homogeneous solution, and the resulting solution was referred to as a raw material liquid C. These solutions were reacted using the reaction apparatus 1 shown in FIG. 1 in the following manner. The raw material liquid A and the raw material liquid B were transferred using diaphragm pumps (manufactured by KNF Co. Ltd.) 35a and 35b, respectively, at a rate of 1.0 ml/min and mixed by a T-shape mixer 15, and the resulting mixture was allowed to flow in a retention line 17 for 1 minutes to prepare a toluene solution of phosgene. Next, the raw material liquid C was transferred using a diaphragm pump (manufactured by KNF Co. Ltd.) 35c at a rate of 2.0 ml/min and mixed with the toluene solution of phosgene that was continuously flowing (2.0 ml/min) by another T-shape mixer 16, and the resulting mixture was allowed to flow in a retention line 18 for 3 minutes to perform a reaction. After the bottles containing the raw material liquid A, the raw material liquid B, and the raw material liquid C was emptied, the reagent in the flow channel was washed and flushed with toluene at the same rate. Note that the T-shape mixers 15 and 16 (inner diameter: 0.5 mm, material: polytetrafluoroethylene (PTFE)) and the retention lines 17 and 18 (inner diameter of tube: 2.0 mm, material: polytetrafluoroethylene (PTFE)) were placed in a constant-temperature bath 31 at 35° C. to carry out this examination experiment. The reaction solution was continuously quenched while stirring with 75.0 g of 18% phosphoric acid aqueous solution in a flask 32. After separation, 100.14 g of an organic layer containing 1.31 g of N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanyl-N-carboxyanhydride was obtained (yield: 80%). No crystals precipitated during the reaction, and the reaction solution was a clear solution. |
| Stage #1: bis(trichloromethyl) carbonate; [1(S)-(ethoxycarbonyl)-3-phenylpropyl]-(S)-alanine In dichloromethane at 20 - 30℃; for 14 - 16h; Heating / reflux; Stage #2: With sodium hydrogencarbonate In water; acetone at 0 - 20℃; for 0.5 - 1.5h; | ||
| Stage #1: bis(trichloromethyl) carbonate; [1(S)-(ethoxycarbonyl)-3-phenylpropyl]-(S)-alanine With disodium hydrogenphosphate In dichloromethane; water at 15 - 20℃; for 1.16667h; Stage #2: With pyridine In dichloromethane; water at 15 - 20℃; for 1h; | 1.A Disodium dihydrogen phosphate dihydrate (177 gms;0.994 moles) was dissolved in water (300 ml) at 35°C and cooled to ambient temperature. Dichloromethane (250 ml) was charged and stirred for 15 mins. N-[1-(S)-ethoxy carbonyl-3- phenyl propyl]-L-alanine (106 gms;0.381 moles) was added to the above solution and the reaction mass was cooled to 15°C. Solution of triphosgene (52.8 gms;0.177 moles) dissolved dichloromethane (40 ml) was added dropwise to the reaction mass in 40 mins at 15-200C. The reaction mass was further stirred for 30 min. Pyridine (0.5 ml; 0.006 moles ) was added and the reaction mass was stirred for 1 hr at 15-200C. The reaction mass was settled and layers were separated. Organic layer was washed with 2N HCI till the neutral pH obtained. The organic layer was further washed with water and dried over sodium sulphate. The solvent was evaporated to residue ( 110 gms). |
| 76 %Chromat. | With tributyl-amine In tetrahydrofuran; toluene at 60℃; for 0.05h; Flow reactor; | |
| 1.25 g | With tributyl-amine In tetrahydrofuran; toluene at 60℃; for 0.05h; | 9 Example 9 To 1.50 g of N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanine, 13.50 g of tetrahydrofuran and 1.09 g of tributylamine were added to prepare a homogeneous solution, and the resulting solution was referred to as solution A. To 0.64 g of triphosgene, 15.50 g of toluene was added to prepare a homogeneous solution, and the resulting solution was referred to as solution B. A T-shape mixer (inner diameter: 2 mm, material: polytetrafluoroethylene (PTFE)) and a retention line (inner diameter of tube: 2 mm, material: polytetrafluoroethylene (PTFE)) were placed in a constant-temperature bath at 60° C. Then, the solution A and the solution B were each transferred using a diaphragm pump (manufactured by KNF Japan Co. Ltd.) at a rate of 2 ml/min and mixed by the T-shape mixer, and the resulting mixture was allowed to flow in the retention line for 3 minutes to perform a reaction (amine/solvent=3.8/100 (weight ratio)). The reaction solution was continuously quenched while stirring with 75.00 g of a 18% phosphoric acid aqueous solution in a flask. After separation, 40.21 g of an organic layer containing 1.25 g of N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanyl-N-carboxylic acid anhydride was obtained (yield: 76%). No crystals precipitated during the reaction, and the reaction solution was a clear solution. |

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| In dichloromethane at 0 - 5℃; for 1h; | 2 Preparation of Trandolapril EXAMPLE 2 Preparation of Trandolapril N-[(S)-1-(ethoxycarbonyl)-3-phenylpropyl]-L-alanine (33 g) was added to a flask with methylene dichloride (500 ml) and cooled to a temperature of about 0° C. N,N'-carbonyl diimidazole (19.16 g) was added to the mixture at the same temperature. The reaction was maintained at a temperature ranging from about 0° C. to about 5° C. for about 1 hour. (2S,3aR,7aS)-perhydroindole-2-carboxylic acid (30 g) of Example 1 was added to the reaction mixture and the reaction temperature was maintained at a temperature ranging from about 0° C. to about 5° C. for an about 2 hours. Methylene dichloride was distilled off and acetic acid (4.19 g) in water (500 ml) was added to the reaction mixture. The aqueous layer was saturated with sodium chloride and the product was extracted continuously with methylene dichloride. Methylene dichloride was then distilled off. The residue was dissolved in isopropyl alcohol (165 ml) and the product was isolated to produce trandolapril (30 g). IR (KBr, cm-1): 3444, 3280, 2973, 2942, 2881, 1735, 1654, 1456, 1367, 1193, 1024, 699. The 1H-NMR (CDCl3): δ 7.2 (s, 5H), 4.4(m,4H), 4.2 (q,2H), 3.6-1.3 (m, 18H), 1.28(d+t,6H). CI Mass (m/z): 429.6(M-H). | |
| With hydrogenchloride In 1,4-dioxane; dichloromethane at 23℃; for 0.015h; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With benzotriazol-1-ol; triethylamine In dichloromethane at 25 - 30℃; for 16h; | 6 Example 6. Preparation of benzyl ramipril; 40 gms of (S,S,S)-2-azabicyclo[3.3.0]-octane-3-carboxylic acid benzyl ester hydrochloride was charged in a round bottom flask to this 40 gms of triethylamine,26gms of l-hydroxybenzotriazole,46 gms of N-[l-(S)-(ethoxy carbonyl)-3-phenylpropyl]-L- alanine, 33 gms of N,N dicyclohexyl carbodimide and 700ml of dichloromethane were added. The reaction mixture was stirred at 25-30° C for 16 hrs. Dicyclohexyl urea precipitated out and was removed by filteration.The filtrate was washed with 1200ml of water followed by distillation of solvent to obtain benzyl ramipril as oil. Yield=71.9gm |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 72 g | With 4-methyl-morpholine; benzotriazol-1-ol; dicyclohexyl-carbodiimide In toluene at 0 - 5℃; for 1h; | 11 Preparation of [2S, 3aS, 6aS]-1-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]octahydrocyclopenta[b]pyrrole-2-carboxylic acid [Ramipril] Toluene (400 ml) was added to 1-hydroxybenzotriazole (26.6 gm) and stirred for 15 minutes. N-(1-S-carbethoxy-3-phenyl propyl)-S-alanine (44 gm) and optically pure hydrochloric acid addition salt of (2S, 3aS, 6aS)-octahydrocyclopenta[b]pyrrole-2-carboxylic acid benzyl ester (40 gms) obtained from example 9 was added to the reaction mixture at 0-5°C. N-methyl morpholine (15.8 gms) was added and the reaction mixture was stirred for 5 minutes. Dicyclohexyl carbodiimide (32.8 gms) was added and the mixture was stirred for 60 minutes at 0-5°C. After completion of the reaction, reaction mass was filtered. Toluene layer was concentrated and acetone (95 ml) was added and mixture was stirred at 0-5°C. The solution was filtered and distilled under vacuum below 40°C. Thick yellow oil (72 gm) of benzyl ester of Ramipril was obtained. Ethanol (640 ml) was added to the ester. 5% Pd/C was added to the reaction mixture and hydrogenation was carried out at 20-22°C at 45-50 psi hydrogen pressure. The mass was filtered and the filtrate was distilled and degassed under vacuum below 25°C. [2S, 3aS, 6aS]-1-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl] octahydrocyclopenta[b] pyrrole-2-carboxylic acid obtained was isolated by DIPE (480 ml) at 0-15°C. The solid was dried at 30°C under vacuum. (wt. on dry basis: 50.2 gms) (Purity: 99.7%; 98.1% ee) |
Tags: 82717-96-2 | NEPA | Amino Acid Derivatives | Carboxylic Acids | Benzene Compounds | N-protective Amino Acid | Organic Building Blocks | Amino Acids | Amino Acids

A1278697 [80828-26-8]
4-[2-(1-Carboxy-ethylamino)-phenyl]-butyric acid ethylester;Hydrochloride
Reason: Free-salt

A184650 [90940-54-8]
D-Homophenylalanine ethyl ester hydrochloride
Similarity: 0.85
Precautionary Statements-General | |
| Code | Phrase |
| P101 | If medical advice is needed,have product container or label at hand. |
| P102 | Keep out of reach of children. |
| P103 | Read label before use |
Prevention | |
| Code | Phrase |
| P201 | Obtain special instructions before use. |
| P202 | Do not handle until all safety precautions have been read and understood. |
| P210 | Keep away from heat/sparks/open flames/hot surfaces. - No smoking. |
| P211 | Do not spray on an open flame or other ignition source. |
| P220 | Keep/Store away from clothing/combustible materials. |
| P221 | Take any precaution to avoid mixing with combustibles |
| P222 | Do not allow contact with air. |
| P223 | Keep away from any possible contact with water, because of violent reaction and possible flash fire. |
| P230 | Keep wetted |
| P231 | Handle under inert gas. |
| P232 | Protect from moisture. |
| P233 | Keep container tightly closed. |
| P234 | Keep only in original container. |
| P235 | Keep cool |
| P240 | Ground/bond container and receiving equipment. |
| P241 | Use explosion-proof electrical/ventilating/lighting/equipment. |
| P242 | Use only non-sparking tools. |
| P243 | Take precautionary measures against static discharge. |
| P244 | Keep reduction valves free from grease and oil. |
| P250 | Do not subject to grinding/shock/friction. |
| P251 | Pressurized container: Do not pierce or burn, even after use. |
| P260 | Do not breathe dust/fume/gas/mist/vapours/spray. |
| P261 | Avoid breathing dust/fume/gas/mist/vapours/spray. |
| P262 | Do not get in eyes, on skin, or on clothing. |
| P263 | Avoid contact during pregnancy/while nursing. |
| P264 | Wash hands thoroughly after handling. |
| P265 | Wash skin thouroughly after handling. |
| P270 | Do not eat, drink or smoke when using this product. |
| P271 | Use only outdoors or in a well-ventilated area. |
| P272 | Contaminated work clothing should not be allowed out of the workplace. |
| P273 | Avoid release to the environment. |
| P280 | Wear protective gloves/protective clothing/eye protection/face protection. |
| P281 | Use personal protective equipment as required. |
| P282 | Wear cold insulating gloves/face shield/eye protection. |
| P283 | Wear fire/flame resistant/retardant clothing. |
| P284 | Wear respiratory protection. |
| P285 | In case of inadequate ventilation wear respiratory protection. |
| P231 + P232 | Handle under inert gas. Protect from moisture. |
| P235 + P410 | Keep cool. Protect from sunlight. |
Response | |
| Code | Phrase |
| P301 | IF SWALLOWED: |
| P304 | IF INHALED: |
| P305 | IF IN EYES: |
| P306 | IF ON CLOTHING: |
| P307 | IF exposed: |
| P308 | IF exposed or concerned: |
| P309 | IF exposed or if you feel unwell: |
| P310 | Immediately call a POISON CENTER or doctor/physician. |
| P311 | Call a POISON CENTER or doctor/physician. |
| P312 | Call a POISON CENTER or doctor/physician if you feel unwell. |
| P313 | Get medical advice/attention. |
| P314 | Get medical advice/attention if you feel unwell. |
| P315 | Get immediate medical advice/attention. |
| P320 | |
| P302 + P352 | IF ON SKIN: wash with plenty of soap and water. |
| P321 | |
| P322 | |
| P330 | Rinse mouth. |
| P331 | Do NOT induce vomiting. |
| P332 | IF SKIN irritation occurs: |
| P333 | If skin irritation or rash occurs: |
| P334 | Immerse in cool water/wrap n wet bandages. |
| P335 | Brush off loose particles from skin. |
| P336 | Thaw frosted parts with lukewarm water. Do not rub affected area. |
| P337 | If eye irritation persists: |
| P338 | Remove contact lenses, if present and easy to do. Continue rinsing. |
| P340 | Remove victim to fresh air and keep at rest in a position comfortable for breathing. |
| P341 | If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. |
| P342 | If experiencing respiratory symptoms: |
| P350 | Gently wash with plenty of soap and water. |
| P351 | Rinse cautiously with water for several minutes. |
| P352 | Wash with plenty of soap and water. |
| P353 | Rinse skin with water/shower. |
| P360 | Rinse immediately contaminated clothing and skin with plenty of water before removing clothes. |
| P361 | Remove/Take off immediately all contaminated clothing. |
| P362 | Take off contaminated clothing and wash before reuse. |
| P363 | Wash contaminated clothing before reuse. |
| P370 | In case of fire: |
| P371 | In case of major fire and large quantities: |
| P372 | Explosion risk in case of fire. |
| P373 | DO NOT fight fire when fire reaches explosives. |
| P374 | Fight fire with normal precautions from a reasonable distance. |
| P376 | Stop leak if safe to do so. Oxidising gases (section 2.4) 1 |
| P377 | Leaking gas fire: Do not extinguish, unless leak can be stopped safely. |
| P378 | |
| P380 | Evacuate area. |
| P381 | Eliminate all ignition sources if safe to do so. |
| P390 | Absorb spillage to prevent material damage. |
| P391 | Collect spillage. Hazardous to the aquatic environment |
| P301 + P310 | IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. |
| P301 + P312 | IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell. |
| P301 + P330 + P331 | IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. |
| P302 + P334 | IF ON SKIN: Immerse in cool water/wrap in wet bandages. |
| P302 + P350 | IF ON SKIN: Gently wash with plenty of soap and water. |
| P303 + P361 + P353 | IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower. |
| P304 + P312 | IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell. |
| P304 + P340 | IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. |
| P304 + P341 | IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. |
| P305 + P351 + P338 | IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. |
| P306 + P360 | IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes. |
| P307 + P311 | IF exposed: call a POISON CENTER or doctor/physician. |
| P308 + P313 | IF exposed or concerned: Get medical advice/attention. |
| P309 + P311 | IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician. |
| P332 + P313 | IF SKIN irritation occurs: Get medical advice/attention. |
| P333 + P313 | IF SKIN irritation or rash occurs: Get medical advice/attention. |
| P335 + P334 | Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages. |
| P337 + P313 | IF eye irritation persists: Get medical advice/attention. |
| P342 + P311 | IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician. |
| P370 + P376 | In case of fire: Stop leak if safe to Do so. |
| P370 + P378 | In case of fire: |
| P370 + P380 | In case of fire: Evacuate area. |
| P370 + P380 + P375 | In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion. |
| P371 + P380 + P375 | In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion. |
Storage | |
| Code | Phrase |
| P401 | |
| P402 | Store in a dry place. |
| P403 | Store in a well-ventilated place. |
| P404 | Store in a closed container. |
| P405 | Store locked up. |
| P406 | Store in corrosive resistant/ container with a resistant inner liner. |
| P407 | Maintain air gap between stacks/pallets. |
| P410 | Protect from sunlight. |
| P411 | |
| P412 | Do not expose to temperatures exceeding 50 oC/ 122 oF. |
| P413 | |
| P420 | Store away from other materials. |
| P422 | |
| P402 + P404 | Store in a dry place. Store in a closed container. |
| P403 + P233 | Store in a well-ventilated place. Keep container tightly closed. |
| P403 + P235 | Store in a well-ventilated place. Keep cool. |
| P410 + P403 | Protect from sunlight. Store in a well-ventilated place. |
| P410 + P412 | Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF. |
| P411 + P235 | Keep cool. |
Disposal | |
| Code | Phrase |
| P501 | Dispose of contents/container to ... |
| P502 | Refer to manufacturer/supplier for information on recovery/recycling |
Physical hazards | |
| Code | Phrase |
| H200 | Unstable explosive |
| H201 | Explosive; mass explosion hazard |
| H202 | Explosive; severe projection hazard |
| H203 | Explosive; fire, blast or projection hazard |
| H204 | Fire or projection hazard |
| H205 | May mass explode in fire |
| H220 | Extremely flammable gas |
| H221 | Flammable gas |
| H222 | Extremely flammable aerosol |
| H223 | Flammable aerosol |
| H224 | Extremely flammable liquid and vapour |
| H225 | Highly flammable liquid and vapour |
| H226 | Flammable liquid and vapour |
| H227 | Combustible liquid |
| H228 | Flammable solid |
| H229 | Pressurized container: may burst if heated |
| H230 | May react explosively even in the absence of air |
| H231 | May react explosively even in the absence of air at elevated pressure and/or temperature |
| H240 | Heating may cause an explosion |
| H241 | Heating may cause a fire or explosion |
| H242 | Heating may cause a fire |
| H250 | Catches fire spontaneously if exposed to air |
| H251 | Self-heating; may catch fire |
| H252 | Self-heating in large quantities; may catch fire |
| H260 | In contact with water releases flammable gases which may ignite spontaneously |
| H261 | In contact with water releases flammable gas |
| H270 | May cause or intensify fire; oxidizer |
| H271 | May cause fire or explosion; strong oxidizer |
| H272 | May intensify fire; oxidizer |
| H280 | Contains gas under pressure; may explode if heated |
| H281 | Contains refrigerated gas; may cause cryogenic burns or injury |
| H290 | May be corrosive to metals |
Health hazards | |
| Code | Phrase |
| H300 | Fatal if swallowed |
| H301 | Toxic if swallowed |
| H302 | Harmful if swallowed |
| H303 | May be harmful if swallowed |
| H304 | May be fatal if swallowed and enters airways |
| H305 | May be harmful if swallowed and enters airways |
| H310 | Fatal in contact with skin |
| H311 | Toxic in contact with skin |
| H312 | Harmful in contact with skin |
| H313 | May be harmful in contact with skin |
| H314 | Causes severe skin burns and eye damage |
| H315 | Causes skin irritation |
| H316 | Causes mild skin irritation |
| H317 | May cause an allergic skin reaction |
| H318 | Causes serious eye damage |
| H319 | Causes serious eye irritation |
| H320 | Causes eye irritation |
| H330 | Fatal if inhaled |
| H331 | Toxic if inhaled |
| H332 | Harmful if inhaled |
| H333 | May be harmful if inhaled |
| H334 | May cause allergy or asthma symptoms or breathing difficulties if inhaled |
| H335 | May cause respiratory irritation |
| H336 | May cause drowsiness or dizziness |
| H340 | May cause genetic defects |
| H341 | Suspected of causing genetic defects |
| H350 | May cause cancer |
| H351 | Suspected of causing cancer |
| H360 | May damage fertility or the unborn child |
| H361 | Suspected of damaging fertility or the unborn child |
| H361d | Suspected of damaging the unborn child |
| H362 | May cause harm to breast-fed children |
| H370 | Causes damage to organs |
| H371 | May cause damage to organs |
| H372 | Causes damage to organs through prolonged or repeated exposure |
| H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
| Code | Phrase |
| H400 | Very toxic to aquatic life |
| H401 | Toxic to aquatic life |
| H402 | Harmful to aquatic life |
| H410 | Very toxic to aquatic life with long-lasting effects |
| H411 | Toxic to aquatic life with long-lasting effects |
| H412 | Harmful to aquatic life with long-lasting effects |
| H413 | May cause long-lasting harmful effects to aquatic life |
| H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
Sorry,this product has been discontinued.
Home
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :
Total Compounds: mg
The concentration of the dissolution solution you need to prepare is mg/mL




